FDA 510(k) Application Details - K202567

Device Classification Name	Test, Amphetamine, Over The Counter   More FDA Info for this Device
510(K) Number	K202567
Device Name	Test, Amphetamine, Over The Counter
Applicant	Guangzhou Wondfo Biotech Co., Ltd. No. 8 Lizhishan Road, Science City Guangzhou 510641 CN Other 510(k) Applications for this Company
Contact	Yi Mei Other 510(k) Applications for this Contact
Regulation Number	862.3100   More FDA Info for this Regulation Number
Classification Product Code	NFT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/04/2020
Decision Date	09/25/2020
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	TX - Clinical Toxicology
Review Advisory Committee	TX - Clinical Toxicology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review